4-(Methylsulfanyl)-10-(1-phenylethyl)-10H-phenoxazine

Base Information

Chemical Name:4-(Methylsulfanyl)-10-(1-phenylethyl)-10H-phenoxazine
CAS No.:113201-95-9
Molecular Formula:C21H19NOS
Molecular Weight:333.454
Hs Code.:
DSSTox Substance ID:DTXSID20559101
Mol file:113201-95-9.mol

Synonyms:113201-95-9;SCHEMBL10558888;DTXSID20559101;4-(METHYLSULFANYL)-10-(1-PHENYLETHYL)-10H-PHENOXAZINE

Suppliers and Price of 4-(Methylsulfanyl)-10-(1-phenylethyl)-10H-phenoxazine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of 4-(Methylsulfanyl)-10-(1-phenylethyl)-10H-phenoxazine

Chemical Property:

XLogP3:5.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:333.11873540
Heavy Atom Count:24
Complexity:411

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C1=CC=CC=C1)N2C3=C(C(=CC=C3)SC)OC4=CC=CC=C42

Technology Process of 4-(Methylsulfanyl)-10-(1-phenylethyl)-10H-phenoxazine

There total 4 articles about 4-(Methylsulfanyl)-10-(1-phenylethyl)-10H-phenoxazine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 624-92-0
Dimethyldisulphide

: 113202-17-8
10-(α-methylbenzyl)phenoxazine

: 135-67-1
phenoxazine

: 113201-95-9
4-(methylthio)-10-(α-methylbenzyl)phenoxazine

: 113202-10-1
4,6-dimethylthio-N-(α-phenylethyl)phenoxazine

Guidance literature:: With n-butyllithium; Yield given. Multistep reaction. Yields of byproduct given; 1.) THF, hexane, 0 deg C, 3 h, 2.) -78 deg C, 15 min;
DOI:10.1021/jo00270a027

Reference yield:

: 113202-18-9
10-(tert-butyldimethylsilyl)-phenoxazine

: 113201-95-9
4-(methylthio)-10-(α-methylbenzyl)phenoxazine

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) n-BuLi / 1.) THF, hexane, 0 deg C, 3 h, 2.) -78 deg C, 15 min

2: 1.) 50percent NaH in mineral oil / 1.) DMF, room temp., 1 h, 2.) DMF, room temp., 0.5 h

3: 1.) n-BuLi / 1.) THF, hexane, 0 deg C, 3 h, 2.) -78 deg C, 15 min

With n-butyllithium; sodium hydride;
DOI:10.1021/jo00270a027

Reference yield:

: 135-67-1
phenoxazine

: 113201-95-9
4-(methylthio)-10-(α-methylbenzyl)phenoxazine

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) 50percent NaH in mineral oil / 1.) DMF, room temp., 1 h, 2.) DMF, room temp., 0.5 h

2: 1.) n-BuLi / 1.) THF, hexane, 0 deg C, 3 h, 2.) -78 deg C, 15 min

With n-butyllithium; sodium hydride;
DOI:10.1021/jo00270a027